HGVS | Genome Assembly |
---|---|
NC_000011.10:g.55811755_55811756insTTT , CM000673.2:g.55811755_55811756insTTT | GRCh38 |
NC_000011.9:g.55579231_55579232insTTT , CM000673.1:g.55579231_55579232insTTT | GRCh37 |
NC_000011.8:g.55335807_55335808insTTT | NCBI36 |
NG_052620.1:g.5389_5390insTTT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000625203.2:c.289_290insTTT MANE Select | ENSP00000485319.1:p.Gly96_Cys97insPhe | |
ENST00000333973.3:c.289_290insTTT | ENSP00000335529.2:p.Gly96_Cys97insPhe | |
ENST00000623450.1:c.289_290insTTT | ENSP00000485509.1:p.Gly96_Cys97insPhe | |
ENST00000625203.1:c.289_290insTTT | ENSP00000485319.1:p.Gly96_Cys97insPhe | |
NM_001004738.1:c.289_290insTTT | NP_001004738.1:p.Gly96_Cys97insPhe | |
NM_001004738.2:c.289_290insTTT MANE Select | NP_001004738.1:p.Gly96_Cys97insPhe |